|
Symbol Name ID |
Cplx1
complexin 1 MGI:104727 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cerebral cortical atrophy |
Cerebral palsy |
EEG with generalized epileptiform discharges |
Absent speech |
Intellectual disability |
Inability to walk |
Epileptic encephalopathy |
Global developmental delay |
Delayed ability to walk |
Seizure |
Bilateral tonic-clonic seizure |
Generalized-onset seizure |
Generalized myoclonic seizure |
Generalized tonic seizure |
Epileptic spasm |
Myoclonic seizure |
| Disease(s) Associated with CPLX1 | ||||||||||||||||
| developmental and epileptic encephalopathy 63 |
| Mouse Phenotypes | sporadic seizures |
abnormal neuron physiology |
decreased excitatory postsynaptic current amplitude |
decreased miniature excitatory postsynaptic current frequency |
abnormal paired-pulse inhibition |
|
| Availability | Mouse Genotype | |||||
| Cplx1tm2Bros/Cplx1tm2Bros | ||||||
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
|
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 04/30/2024 MGI 6.23 |
|
|
|
||
Analysis Tools